US12576094B2ActiveUtilityA1
Combination cannabinoid-phenylethanoid formulation for treatment of inflammation and methods related thereto
Est. expiryNov 20, 2039(~13.4 yrs left)· nominal 20-yr term from priority
A61K 31/658A61K 36/3482A61K 31/216A61P 29/00A61K 45/06A61K 9/00A61P 19/02A61K 31/222A61K 36/63
41
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Cited by
27
References
18
Claims
Abstract
The present invention describes cannabinoid formulations that combine cannabinoids, such as CBD, with other active agents within the phenylethanoid class of compounds, such as oleocanthal, which, in combination, provide synergistic anti-inflammatory effects. These combination preparations are capable of increasing anti-inflammatory effects when compared to each individual compound alone, and are further capable of delivery through a variety of administration routes.
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A composition for treatment of inflammatory conditions in an animal, said composition comprising:
at least one cannabinoid; and at least one phenylethanoid;
wherein said composition is capable of having an anti-inflammatory effect when administered to an animal, and
wherein the at least one phenylethanoid comprises oleocanthal.
2 . The composition of claim 1 , wherein the molar ratio of the at least one cannabinoid and the at least one phenylethanoid is between 10:1 and 1:10.
3 . The composition of claim 1 , wherein the molar ratio of the at least one cannabinoid and the at least one phenylethanoid is between 5:1 and 1:5.
4 . The composition of claim 1 , wherein the molar ratio of the at least one cannabinoid and the at least one phenylethanoid is substantially 1:1.
5 . The composition of claim 1 , wherein said composition is suitable for administration selected from a group consisting of: oral administration, topical administration, mucosal administration, pulmonary administration, subcutaneous administration, intravenous administration, intraperitoneal administration, suppository administration, and intramuscular administration.
6 . The composition of claim 1 , wherein said composition is a formulation selected from a group consisting of: a tablet, capsule, spray, drop, solution, suspension, gel, ointment, lotion, cream, powder, transdermal patch, tampon, or a sponge.
7 . The composition of claim 1 , wherein the at least one phenylethanoid is selected from the group consisting of: olive oil, oleocanthal, tyrosol, hydroxytyrosol, and combinations thereof.
8 . The composition of claim 1 , wherein the cannabinoid is cannabidiol (CBD).
9 . The composition of claim 1 , wherein the cannabinoid is selected from the group consisting of: cannabidiol (CBD), cannabidivarol (CBDV), cannabinol (CBN), cannabigerol (CBG), cannabivarol (CBV), cannabicyclol (CBL), tetrahydrocannabinol (THC), tetrahydrocannabinol-C4, (THC-C4), tetrahydrocannabivarin (THCV), 11-Hydroxy-49-tetrahydrocannabinol, (11-OH-THC), 11-nor-9-Carboxy-Δ9-tetrahydrocannabinol, and combinations thereof.
10 . A method for preparing a combination formulation having anti-inflammatory properties, the method comprising the steps of:
providing at least one cannabinoid; providing at least one phenylethanoid, wherein the at least one phenylethanoid comprises oleocanthal; and
combining the at least one cannabinoid and the at least one phenylethanoid to form a combination formulation;
wherein said combination formulation is capable of reducing inflammation in an animal administered said combination formulation.
11 . The method of claim 10 , wherein a molar ratio of the at least one cannabinoid and the at least one phenylethanoid in the combination formulation is between 10:1 and 1:10.
12 . The method of claim 10 , wherein a molar ratio of the at least one cannabinoid and the at least one phenylethanoid in the combination formulation is between 5:1 and 1:5.
13 . The method of claim 10 , wherein a molar ratio of the at least one cannabinoid and the at least one phenylethanoid in the combination formulation is substantially 1:1.
14 . The method of claim 10 , wherein said combination formulation is suitable for administration selected from a group consisting of: oral administration, topical administration, mucosal administration, pulmonary administration, subcutaneous administration, intravenous administration, intraperitoneal administration, suppository administration, and intramuscular administration.
15 . The method of claim 10 , wherein said combination formulation is a formulation selected from the group consisting of: a tablet, capsule, spray, drop, solution, suspension, gel, ointment, lotion, cream, powder, transdermal patch, tampon, or a sponge.
16 . The method of claim 10 , wherein the at least one phenylethanoid is selected from a group consisting of: olive oil, oleocanthal, tyrosol, hydroxytyrosol, and combinations thereof.
17 . The method of claim 10 , wherein the cannabinoid is cannabidiol (CBD).
18 . The method of claim 10 , wherein the cannabinoid is selected from the group consisting of: cannabidiol (CBD), cannabidivarol (CBDV), cannabinol (CBN), cannabigerol (CBG), cannabivarol (CBV), cannabicyclol (CBL), tetrahydrocannabinol (THC), tetrahydrocannabinol-C4, (THC-C4), tetrahydrocannabivarin (THCV), 11-Hydroxy-49-tetrahydrocannabinol, (11-OH-THC), 11-nor-9-Carboxy-Δ9-tetrahydrocannabinol, and combinations thereof.Cited by (0)
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